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Seasonal cycling in the gut microbiome of the Hadza hunter-gatherers of Tanzania.坦桑尼亚哈扎族狩猎采集者肠道微生物群的季节性循环。
Science. 2017 Aug 25;357(6353):802-806. doi: 10.1126/science.aan4834.
2
Protective Factors in the Intestinal Microbiome Against Clostridium difficile Infection in Recipients of Allogeneic Hematopoietic Stem Cell Transplantation.异基因造血干细胞移植受者肠道微生物群中抵抗艰难梭菌感染的保护因素
J Infect Dis. 2017 Apr 1;215(7):1117-1123. doi: 10.1093/infdis/jix011.
3
Microbiota Disruption Induced by Early Use of Broad-Spectrum Antibiotics Is an Independent Risk Factor of Outcome after Allogeneic Stem Cell Transplantation.早期使用广谱抗生素引起的微生物群破坏是异基因造血干细胞移植后预后的独立危险因素。
Biol Blood Marrow Transplant. 2017 May;23(5):845-852. doi: 10.1016/j.bbmt.2017.02.006. Epub 2017 Feb 14.
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Effect of Fecal Microbiota Transplantation on Recurrence in Multiply Recurrent Clostridium difficile Infection: A Randomized Trial.粪便微生物群移植对多次复发性艰难梭菌感染复发的影响:一项随机试验
Ann Intern Med. 2016 Nov 1;165(9):609-616. doi: 10.7326/M16-0271. Epub 2016 Aug 23.
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Fecal microbiota transplantation for patients with steroid-resistant acute graft-versus-host disease of the gut.粪便微生物群移植用于肠道类固醇难治性急性移植物抗宿主病患者。
Blood. 2016 Oct 20;128(16):2083-2088. doi: 10.1182/blood-2016-05-717652. Epub 2016 Jul 26.
6
Increased GVHD-related mortality with broad-spectrum antibiotic use after allogeneic hematopoietic stem cell transplantation in human patients and mice.在人类患者和小鼠接受异基因造血干细胞移植后,使用广谱抗生素会增加移植物抗宿主病(GVHD)相关死亡率。
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Resurrecting the intestinal microbiota to combat antibiotic-resistant pathogens.重塑肠道微生物群以对抗抗生素耐药病原体。
Science. 2016 Apr 29;352(6285):535-8. doi: 10.1126/science.aad9382.
8
The gut microbiota and host health: a new clinical frontier.肠道微生物群与宿主健康:一个新的临床前沿领域。
Gut. 2016 Feb;65(2):330-9. doi: 10.1136/gutjnl-2015-309990. Epub 2015 Sep 2.
9
Low urinary indoxyl sulfate levels early after transplantation reflect a disrupted microbiome and are associated with poor outcome.移植后早期尿吲哚硫酸水平较低反映了微生物群的紊乱,并与不良预后相关。
Blood. 2015 Oct 1;126(14):1723-8. doi: 10.1182/blood-2015-04-638858. Epub 2015 Jul 24.
10
Error filtering, pair assembly and error correction for next-generation sequencing reads.下一代测序reads 的错误过滤、配对组装和纠错。
Bioinformatics. 2015 Nov 1;31(21):3476-82. doi: 10.1093/bioinformatics/btv401. Epub 2015 Jul 2.

通过自体粪便微生物群移植重建抗生素治疗患者的肠道微生物群。

Reconstitution of the gut microbiota of antibiotic-treated patients by autologous fecal microbiota transplant.

机构信息

Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

Department of Zoology, University of Oxford, Oxford, UK.

出版信息

Sci Transl Med. 2018 Sep 26;10(460). doi: 10.1126/scitranslmed.aap9489.

DOI:10.1126/scitranslmed.aap9489
PMID:30257956
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6468978/
Abstract

Antibiotic treatment can deplete the commensal bacteria of a patient's gut microbiota and, paradoxically, increase their risk of subsequent infections. In allogeneic hematopoietic stem cell transplantation (allo-HSCT), antibiotic administration is essential for optimal clinical outcomes but significantly disrupts intestinal microbiota diversity, leading to loss of many beneficial microbes. Although gut microbiota diversity loss during allo-HSCT is associated with increased mortality, approaches to reestablish depleted commensal bacteria have yet to be developed. We have initiated a randomized, controlled clinical trial of autologous fecal microbiota transplantation (auto-FMT) versus no intervention and have analyzed the intestinal microbiota profiles of 25 allo-HSCT patients (14 who received auto-FMT treatment and 11 control patients who did not). Changes in gut microbiota diversity and composition revealed that the auto-FMT intervention boosted microbial diversity and reestablished the intestinal microbiota composition that the patient had before antibiotic treatment and allo-HSCT. These results demonstrate the potential for fecal sample banking and posttreatment remediation of a patient's gut microbiota after microbiota-depleting antibiotic treatment during allo-HSCT.

摘要

抗生素治疗会消耗患者肠道微生物群中的共生细菌,而这却反常地增加了他们随后感染的风险。在异基因造血干细胞移植(allo-HSCT)中,抗生素的使用对于获得最佳临床效果至关重要,但它会显著破坏肠道微生物多样性,导致许多有益微生物的丧失。虽然 allo-HSCT 期间肠道微生物多样性的丧失与死亡率增加有关,但恢复耗尽的共生细菌的方法尚未开发出来。我们已经启动了一项自体粪便微生物群移植(auto-FMT)与无干预对照的随机临床试验,并对 25 例 allo-HSCT 患者的肠道微生物群谱进行了分析(14 例接受了 auto-FMT 治疗,11 例对照患者未接受治疗)。肠道微生物多样性和组成的变化表明,auto-FMT 干预措施提高了微生物多样性,并重建了患者在抗生素治疗和 allo-HSCT 之前的肠道微生物群组成。这些结果表明,在 allo-HSCT 期间使用消耗微生物群的抗生素治疗后,粪便样本库和治疗后对患者肠道微生物群的修复具有潜在应用价值。